Clinical pilot study on forced orthodontic extrusion for restoration of deeply destroyed teeth
- Conditions
- K08.3Retained dental root
- Registration Number
- DRKS00026697
- Lead Sponsor
- Charité Campus Benjamin Franklin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
men, women, 18 years and older
the patient is informed about recall sessions
patients with a deeply destroyed tooth in a closed row of teeth
probing depths prospective crown-to-root ratio good compliance
Exclusion Criteria
longitudinal fracture, >/= 2 missing teeth and shortened dental arch, probing depths > 3 mm at decay level, prospective crown-to-root ratio > 1:1, mobility grade >/= II, poor compliance, poor oral hygiene
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The survival rate after five years serves as the primary endpoint of this clinical study.
- Secondary Outcome Measures
Name Time Method The periodontal and clinical situation after five years of function serves as the secondary endpoint of this clinical study.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie orthodontic extrusion for root retention in K08.3 cases?
How does forced orthodontic extrusion compare to endodontic retreatment for deeply destroyed teeth?
Are there specific biomarkers that predict successful orthodontic extrusion outcomes in retained roots?
What are the potential adverse events associated with orthodontic extrusion techniques in dental restoration?
What combination therapies enhance orthodontic extrusion effectiveness for root retention compared to standalone approaches?